It depends on the specific situation. Generally speaking, the informed consent form of clinical trials needs to provide detailed research information so that subjects can make informed decisions. For ethnic minority subjects, it may be necessary to provide information that is easy to understand in their language or cultural traditions to ensure that they can truly understand and voluntarily participate in the research. However, whether it is necessary to provide special informed consent of ethnic minorities may need to be decided according to specific clinical trials and research designs.
Please note that the above information is for reference only. If you have any specific questions about clinical trials, it is recommended to consult professionals or relevant institutions.